Division of Viral Diseases, National Center for Immunization and Respiratory Diseases, Centers for Disease Control and Prevention, Atlanta, Georgia, USA.
J Virol. 2013 May;87(9):4907-22. doi: 10.1128/JVI.02954-12. Epub 2013 Feb 13.
Since 2005, a large poliomyelitis outbreak associated with type 2 circulating vaccine-derived poliovirus (cVDPV2) has occurred in northern Nigeria, where immunization coverage with trivalent oral poliovirus vaccine (tOPV) has been low. Phylogenetic analysis of P1/capsid region sequences of isolates from each of the 403 cases reported in 2005 to 2011 resolved the outbreak into 23 independent type 2 vaccine-derived poliovirus (VDPV2) emergences, at least 7 of which established circulating lineage groups. Virus from one emergence (lineage group 2005-8; 361 isolates) was estimated to have circulated for over 6 years. The population of the major cVDPV2 lineage group expanded rapidly in early 2009, fell sharply after two tOPV rounds in mid-2009, and gradually expanded again through 2011. The two major determinants of attenuation of the Sabin 2 oral poliovirus vaccine strain (A481 in the 5'-untranslated region [5'-UTR] and VP1-Ile143) had been replaced in all VDPV2 isolates; most A481 5'-UTR replacements occurred by recombination with other enteroviruses. cVDPV2 isolates representing different lineage groups had biological properties indistinguishable from those of wild polioviruses, including efficient growth in neuron-derived HEK293 cells, the capacity to cause paralytic disease in both humans and PVR-Tg21 transgenic mice, loss of the temperature-sensitive phenotype, and the capacity for sustained person-to-person transmission. We estimate from the poliomyelitis case count and the paralytic case-to-infection ratio for type 2 wild poliovirus infections that ∼700,000 cVDPV2 infections have occurred during the outbreak. The detection of multiple concurrent cVDPV2 outbreaks in northern Nigeria highlights the risks of cVDPV emergence accompanying tOPV use at low rates of coverage in developing countries.
自 2005 年以来,尼日利亚北部发生了与 2 型循环疫苗衍生脊髓灰质炎病毒(cVDPV2)相关的大规模脊髓灰质炎疫情,该地区三价口服脊髓灰质炎疫苗(tOPV)的免疫覆盖率较低。对 2005 年至 2011 年报告的 403 例病例的 P1/衣壳区序列进行系统进化分析,将疫情分为 23 个独立的 2 型疫苗衍生脊髓灰质炎病毒(VDPV2)暴发,其中至少 7 个建立了循环谱系群。来自一次暴发(谱系群 2005-8;361 个分离株)的病毒估计已经传播了 6 年以上。主要的 cVDPV2 谱系群的人群在 2009 年初迅速扩大,在 2009 年中期两轮 tOPV 之后急剧下降,并在 2011 年逐渐再次扩大。Sabin 2 口服脊髓灰质炎疫苗株(5'-非翻译区[5'-UTR]中的 A481 和 VP1-Ile143)衰减的两个主要决定因素在所有 VDPV2 分离株中均已被取代;大多数 A481 5'-UTR 取代是通过与其他肠道病毒重组发生的。代表不同谱系群的 cVDPV2 分离株具有与野生脊灰病毒相同的生物学特性,包括在神经元衍生的 HEK293 细胞中的高效生长、在人和 PVR-Tg21 转基因小鼠中引起麻痹性疾病的能力、丧失温度敏感表型的能力以及持续人际传播的能力。我们根据脊灰病例数和 2 型野生脊灰病毒感染的麻痹病例与感染比估计,在疫情期间发生了约 70 万例 cVDPV2 感染。在尼日利亚北部发现多个同时发生的 cVDPV2 暴发,突显了在发展中国家 tOPV 覆盖率较低的情况下,cVDPV 出现的风险。